| Towards vqa models that can read A Singh, V Natarajan, M Shah, Y Jiang, X Chen, D Batra, D Parikh, ... Proceedings of the IEEE/CVF conference on computer vision and pattern …, 2019 | 926 | 2019 |
| Pythia v0. 1: the winning entry to the vqa challenge 2018 Y Jiang, V Natarajan, X Chen, M Rohrbach, D Batra, D Parikh arXiv preprint arXiv:1807.09956, 2018 | 235 | 2018 |
| Mmf: A multimodal framework for vision and language research A Singh, V Goswami, V Natarajan, Y Jiang, X Chen, M Shah, M Rohrbach, ... MMF: A Multimodal Framework for Vision and Language Research, 2020 | 86 | 2020 |
| Pisces: An accurate and versatile single sample somatic and germline variant caller T Dunn, G Berry, D Emig-Agius, Y Jiang, A Iyer, N Udar, M Strömberg Proceedings of the 8th ACM International Conference on Bioinformatics …, 2017 | 78* | 2017 |
| Pythia-a platform for vision & language research A Singh, V Natarajan, Y Jiang, X Chen, M Shah, M Rohrbach, D Batra, ... SysML Workshop, NeurIPS 2018, 2018 | 70 | 2018 |
| Incorporating functional information in tests of excess de novo mutational load Y Jiang, Y Han, S Petrovski, K Owzar, DB Goldstein, AS Allen The American Journal of Human Genetics 97 (2), 272-283, 2015 | 33 | 2015 |
| Utilizing population controls in rare-variant case-parent association tests Y Jiang, GA Satten, Y Han, MP Epstein, EL Heinzen, DB Goldstein, ... The American Journal of Human Genetics 94 (6), 845-853, 2014 | 22 | 2014 |
| MMF: a multimodal framework for vision and language research (2020) A Singh, V Goswami, V Natarajan, Y Jiang, X Chen, M Shah, M Rohrbach, ... URL: https://github. com/facebookresearch/mmf, 0 | 11 | |
| Testing the Effect of Rare Compound‐Heterozygous and Recessive Mutations in Case–Parent Sequencing Studies Y Jiang, JM McCarthy, AS Allen Genetic epidemiology 39 (3), 166-172, 2015 | 9 | 2015 |
| Nirvana: clinical grade variant annotator M Stromberg, R Roy, J Lajugie, Y Jiang, H Li, E Margulies Proceedings of the 8th ACM International Conference on Bioinformatics …, 2017 | 7 | 2017 |
| Application of rare variant transmission disequilibrium tests to epileptic encephalopathy trio sequence data EPG Project, Epi4K Consortium, EuroEPINOMICS-RES Consortium European Journal of Human Genetics 25 (7), 894, 2017 | 6 | 2017 |
| Leveraging population information in family‐based rare variant association analyses of quantitative traits Y Jiang, Y Ji, AB Sibley, YJ Li, AS Allen Genetic Epidemiology 41 (2), 98-107, 2017 | 4 | 2017 |
| Facilitating the calculation of the efficient score using symbolic computing A B. Sibley, Z Li, Y Jiang, YJ Li, C Chan, A Allen, K Owzar The American Statistician 72 (2), 199-205, 2018 | 1 | 2018 |
| Efficient estimation of grouped survival models Z Li, J Lin, AB Sibley, T Truong, KC Chua, Y Jiang, J McCarthy, DL Kroetz, ... BMC bioinformatics 20, 1-11, 2019 | | 2019 |
